XK Antibody
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中文名稱：XK兔多克隆抗體
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貨號：CSB-PA992680
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規(guī)格：￥1100
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圖片：
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Gel: 8%SDS-PAGE, Lysate: 40 μg, Lane 1-2: Human placenta and normal liver tissue, Primary antibody: CSB-PA992680(XK Antibody) at dilution 1/400 dilution, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 1 minute
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其他：
產(chǎn)品詳情
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Uniprot No.：
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基因名：XK
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別名：XK antibody; XKR1 antibody; XRG1 antibody; Membrane transport protein XK antibody; Kell complex 37 kDa component antibody; Kx antigen antibody; XK-related protein 1 antibody
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宿主：Rabbit
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反應(yīng)種屬：Human
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免疫原：Synthetic peptide of Human XK
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免疫原種屬：Homo sapiens (Human)
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標(biāo)記方式：Non-conjugated
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抗體亞型：IgG
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純化方式：Antigen affinity purification
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
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產(chǎn)品提供形式：Liquid
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應(yīng)用范圍：ELISA,WB
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推薦稀釋比：
Application Recommended Dilution ELISA 1:1000-1:2000 WB 1:200-1:1000 -
Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情
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功能：May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.
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基因功能參考文獻：
- the expression of KX is critical to normal morphology, and null mutations are associated with the McLeod neuroacanthocytosis syndrome. PMID: 26308465
- The XK gene was not linked to hypermutability in red cells from patients with paroxysmal nocturnal hemoglobinuria. PMID: 24816235
- study reports the clinical findings and a novel nonsense hemizygous mutation, c.154C>T (p.Gln52X) at exon 1 of XK gene in a Taiwanese family with McLeod syndrome PMID: 24635891
- Novel XK protein mutations are reported in two patients who exhibit typical clinical characteristics of McLeod syndrome. PMID: 21463873
- This study identified one non-synonymous and one intron variant in mood disorder and schizophrenia subjects, respectively, in XK. PMID: 21145924
- In human cortex, the results show expression of XK in cortical neurons with an apparent cytoplasmic localization. PMID: 17379193
- Sequence analysis demonstrated a 5 bp deletion in exon 2 of the XK gene in McLeod syndrome. PMID: 17469188
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相關(guān)疾病：McLeod syndrome (MLS)
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亞細胞定位：Cell membrane; Multi-pass membrane protein.
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蛋白家族：XK family
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組織特異性：High levels in skeletal muscle, heart, brain, and pancreas; low levels in placenta, lung, liver, and kidney.
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數(shù)據(jù)庫鏈接：
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